Imprinting-Mutation Mechanisms in Prader-Willi Syndrome-Reference-Cited by-同舟云学术

Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

Published:1999-02 Issue:2 Volume:64 Page:397-413
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ohta T.,Gray T.A.,Rogan P.K.,Buiting K.,Gabriel J.M.,Saitoh S.,Muralidhar B.,Bilienska B.,Krajewska-Walasek M.,Driscoll D.J.,Horsthemke B.,Butler M.G.,Nicholls R.D.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference51 articles.

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3. Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint switch models, genetic counseling, and prenatal diagnosis;Buiting;Am J Hum Genet,1998

4. Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting center on human chromosome 15;Buiting;Nat Genet,1995

5. Different mechanisms and recurrence risks of imprinting defects in Angelman syndrome;Bürger;Am J Hum Genet,1997

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